iRhythm Technologies, Inc. seeks a Supervisor, Post‑Market Complaints to lead international complaint investigators and ensure timely, high‑quality evaluations in line with ISO 13485, FDA 21 CFR 820, and MDR guidance.

You will coach the team, manage workload, and drive continuous process improvements. The role partners with Quality leadership and cross‑functional teams to ensure inspection readiness and regulatory compliance across post‑market activities.